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Enhanced Keratinocyte Proliferation and Migration in Co-culture with Fibroblasts
Wound healing is primarily controlled by the proliferation and migration of keratinocytes and fibroblasts as well as the complex interactions between these two cell types. To investigate the interactions between keratinocytes and fibroblasts and the effects of direct cell-to-cell contact on the prol...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3401236/ https://www.ncbi.nlm.nih.gov/pubmed/22911722 http://dx.doi.org/10.1371/journal.pone.0040951 |
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author | Wang, Zhenxiang Wang, Ying Farhangfar, Farhang Zimmer, Monica Zhang, Yongxin |
author_facet | Wang, Zhenxiang Wang, Ying Farhangfar, Farhang Zimmer, Monica Zhang, Yongxin |
author_sort | Wang, Zhenxiang |
collection | PubMed |
description | Wound healing is primarily controlled by the proliferation and migration of keratinocytes and fibroblasts as well as the complex interactions between these two cell types. To investigate the interactions between keratinocytes and fibroblasts and the effects of direct cell-to-cell contact on the proliferation and migration of keratinocytes, keratinocytes and fibroblasts were stained with different fluorescence dyes and co-cultured with or without transwells. During the early stage (first 5 days) of the culture, the keratinocytes in contact with fibroblasts proliferated significantly faster than those not in contact with fibroblasts, but in the late stage (11(th) to 15(th) day), keratinocyte growth slowed down in all cultures unless EGF was added. In addition, keratinocyte migration was enhanced in co-cultures with fibroblasts in direct contact, but not in the transwells. Furthermore, the effects of the fibroblasts on keratinocyte migration and growth at early culture stage correlated with heparin-binding EGF-like growth factor (HB-EGF), IL-1α and TGF-β1 levels in the cultures where the cells were grown in direct contact. These effects were inhibited by anti-HB-EGF, anti-IL-1α and anti-TGF-β1 antibodies and anti-HB-EGF showed the greatest inhibition. Co-culture of keratinocytes and IL-1α and TGF-β1 siRNA-transfected fibroblasts exhibited a significant reduction in HB-EGF production and keratinocyte proliferation. These results suggest that contact with fibroblasts stimulates the migration and proliferation of keratinocytes during wound healing, and that HB-EGF plays a central role in this process and can be up-regulated by IL-1α and TGF-β1, which also regulate keratinocyte proliferation differently during the early and late stage. |
format | Online Article Text |
id | pubmed-3401236 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-34012362012-07-30 Enhanced Keratinocyte Proliferation and Migration in Co-culture with Fibroblasts Wang, Zhenxiang Wang, Ying Farhangfar, Farhang Zimmer, Monica Zhang, Yongxin PLoS One Research Article Wound healing is primarily controlled by the proliferation and migration of keratinocytes and fibroblasts as well as the complex interactions between these two cell types. To investigate the interactions between keratinocytes and fibroblasts and the effects of direct cell-to-cell contact on the proliferation and migration of keratinocytes, keratinocytes and fibroblasts were stained with different fluorescence dyes and co-cultured with or without transwells. During the early stage (first 5 days) of the culture, the keratinocytes in contact with fibroblasts proliferated significantly faster than those not in contact with fibroblasts, but in the late stage (11(th) to 15(th) day), keratinocyte growth slowed down in all cultures unless EGF was added. In addition, keratinocyte migration was enhanced in co-cultures with fibroblasts in direct contact, but not in the transwells. Furthermore, the effects of the fibroblasts on keratinocyte migration and growth at early culture stage correlated with heparin-binding EGF-like growth factor (HB-EGF), IL-1α and TGF-β1 levels in the cultures where the cells were grown in direct contact. These effects were inhibited by anti-HB-EGF, anti-IL-1α and anti-TGF-β1 antibodies and anti-HB-EGF showed the greatest inhibition. Co-culture of keratinocytes and IL-1α and TGF-β1 siRNA-transfected fibroblasts exhibited a significant reduction in HB-EGF production and keratinocyte proliferation. These results suggest that contact with fibroblasts stimulates the migration and proliferation of keratinocytes during wound healing, and that HB-EGF plays a central role in this process and can be up-regulated by IL-1α and TGF-β1, which also regulate keratinocyte proliferation differently during the early and late stage. Public Library of Science 2012-07-20 /pmc/articles/PMC3401236/ /pubmed/22911722 http://dx.doi.org/10.1371/journal.pone.0040951 Text en Wang et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Wang, Zhenxiang Wang, Ying Farhangfar, Farhang Zimmer, Monica Zhang, Yongxin Enhanced Keratinocyte Proliferation and Migration in Co-culture with Fibroblasts |
title | Enhanced Keratinocyte Proliferation and Migration in Co-culture with Fibroblasts |
title_full | Enhanced Keratinocyte Proliferation and Migration in Co-culture with Fibroblasts |
title_fullStr | Enhanced Keratinocyte Proliferation and Migration in Co-culture with Fibroblasts |
title_full_unstemmed | Enhanced Keratinocyte Proliferation and Migration in Co-culture with Fibroblasts |
title_short | Enhanced Keratinocyte Proliferation and Migration in Co-culture with Fibroblasts |
title_sort | enhanced keratinocyte proliferation and migration in co-culture with fibroblasts |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3401236/ https://www.ncbi.nlm.nih.gov/pubmed/22911722 http://dx.doi.org/10.1371/journal.pone.0040951 |
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